Fluorometric study on the amine-catalysed Suzuki–Miyaura coupling
Author:
Funder
National Science Foundation
Publisher
Springer Science and Business Media LLC
Subject
Process Chemistry and Technology,Biochemistry,Bioengineering,Catalysis
Link
https://www.nature.com/articles/s41929-021-00711-0.pdf
Reference17 articles.
1. Miyaura, N. & Suzuki, A. Palladium-catalyzed cross-coupling reactions of organoboron compounds. Chem. Rev. 95, 2457–2483 (1995).
2. Leadbeater, N. E. & Marco, M. Transition-metal-free Suzuki-type coupling reactions: scope and limitations of the methodology. J. Org. Chem. 68, 5660–5667 (2003).
3. Leadbeater, N. E., Marco, M. & Tominack, B. J. First examples of transition-metal free Sonogashira-type couplings. Org. Lett. 5, 3919–3922 (2003).
4. Thathagar, M. B., Beckers, J. & Rothenberg, G. Palladium-free and ligand-free Sonogashira cross-coupling. Green Chem. 6, 215–218 (2004).
5. Arvela, R. K. et al. A reassessment of the transition-metal free Suzuki-type coupling methodology. J. Org. Chem. 70, 161–168 (2005).
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